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  • 1
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 61 (1996), S. 675-683 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Birch wood meal has been phenolated in the presence of oxalic acid alone or its mixture with hydrochloric acid (HCl) at various temperatures ranging from 150 to 250°C under high pressure. The effects of high temperature, high pressure, and the addition of HCl in conjunction with oxalic acid on the amounts of wood residue and combined phenol have been investigated. In the case of the oxalic acid-catalyzed process, by increasing reaction temperature from 180 to 250°C, the amounts of wood residue could be considerably reduced, but the amount of combined phenol decreased. In comparison to a noncatalyzed process in the absence of water, the catalyzed one offered a relatively lower amount of wood residue and a higher amount of combined phenol. However, compared to a noncatalyzed process with water, particularly at a high temperature of 250°C, the catalyzed process gave significantly larger amounts of wood residue. In addition, with a small addition of HCl to an oxalic acid catalyzed system, the amount of wood residue was remarkably reduced compared to that of oxalic acid alone, and the amount of combined phenol could be increased significantly. Furthermore, the mechanical properties of the moldings prepared from the phenolated wood were sufficiently improved by the addition of a small amount of HCl to the oxalic acid-catalyzed system. © 1996 John Wiley & Sons, Inc.
    Additional Material: 16 Ill.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1437-7772
    Keywords: Key words Cisplatin ; Natural killer cell activity ; Natural killer suppressive factor ; Peritoneal cavity ; Intraperitoneal chemotherapy
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract Background. Intraperitoneal (i.p.) chemotherapy is frequently utilized in patients with advanced gastric cancer or peritoneal dissemination. We investigated whether i.p. administration of cisplatin at high or low doses would impair host local immunity with respect to the induction of natural killer (NK) cell suppressive factor in the murine peritoneal cavity. Methods. Cisplatin was administered at a total dose of 10 mg/kg according to two schedules: high-dose bolus injection (HB; 10 mg/kg) and low-dose consecutive injections (LC; 2 mg/kg daily for 5 days). The supernatant obtained from the peritoneal lavage fluid was added during normal splenocyte-mediated NK cytotoxicity assay. The phenotypes of peritoneal exudate cells were analyzed using anti-F4/80 monoclonal antibody (MAb) and anti-I-A MAb. Results. NK cell activity was significantly inhibited by the supernatant obtained from the HB group 7 days after the administration of cisplatin (40.6% of NK cell activity in controls; P 〈 0.05). This inhibition was partly restored by prostaglandin E2 (PGE2) antiserum (69.5% of NK cell activity in controls). NK cell activity was not inhibited at any point by exposure to the supernatant of the LC group. I-A− peritoneal macrophages were more abundant in the HB group than in the LC group (2.9 × 106 vs 4.6 × 105 on day 3; P 〈 0.05). Conclusion. These results suggest that intraperitoneal bolus administration of high-dose cisplatin induces NK suppressive factors, including PGE2, in the peritoneal cavity, whereas low-dose consecutive administration does not.
    Type of Medium: Electronic Resource
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